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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866253Generated: October 29, 2026

Dicyclohexylcarbodiimide → 2-[4-[2-(2H-tetrazol-5-yl)benzamido]-1H-benzimidazol-1-yl]octanoic acid

https://huagongshe.com/reaction/866253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-(1H-1,2,3,4-tetrazol-5-yl)benzoic acidHCID 555192—
ReactantEthyl 2-(4-nitro-1H-benzimidazol-1-yl)octanoateHCID 21468887—
ReactantHCID 178418300HCID 178418300—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product2-[4-[2-(2H-tetrazol-5-yl)benzamido]-1H-benzimidazol-1-yl]octanoic acidHCID 214689909.6%

Reaction Steps

Ethyl 2-(4-nitro-1H-benzimidazol-1-yl)octanoate (4.44 mmoles, 1.48 g.) was hydrogenated over 0.6 g of 5% Pd/C in 100 ml ethanol. The catalyst was filtered over celite. The solution was concentrated. The residue was dissolved in 25 ml DHF and added to a stirred mixture of 2-(2H-tetrazol-5-yl)benzoic acid (4.21 mmoles, 0.80 g), dicyclohexylcarbodiimide (4.31 mmoles, 0.89 g.), and hydroxybenzotriazole (4.44 mmoles, 0.60 g) in 50 ml DMF. The reaction was stirred for 4 hours. The solid was removed by filtration. The reaction was concentrated. The residue was dissolved in ethyl acetate, and washed with water. The pH was adjusted to 8.0 using 5N NaOH. The aqueous layer was acidified to pH 2.5 using 2N HCL, and then extracted with ethyl acetate. The organic phase was separated, washed with water, dried and concentrated. The product was purified over silica gel eluted with 2% EtOH in ethyl acetate with 1% acetic acid to yield 0.18 g of 2-[4-[2-(2H-tetrazol-5-yl)benzamido]-1H-benzimidazol-1-yl]octanoic acid. (MS)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569768
Source datasetuspto-grants-1996_10
ORD IDord-3851f5b3a7f3401692f2c38252b38375
Source noteuspto-grants-1996_10